List of variants in gene DOLK studied for Congenital disorder of glycosylation type 1M

Minimum submission review status:		Collection method:
Minimum conflict level:
Gene type:		Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 77

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HGVS	dbSNP
NC_000009.11:g.(?_131707946)_(131709602_?)dup
NM_014908.3(DOLK):c.101T>C (p.Ile34Thr)	rs1554826863
NM_014908.3(DOLK):c.1067G>A (p.Arg356Gln)	rs199535796
NM_014908.3(DOLK):c.1079A>G (p.Tyr360Cys)	rs138453255
NM_014908.3(DOLK):c.1087G>A (p.Ala363Thr)
NM_014908.3(DOLK):c.1114T>A (p.Phe372Ile)	rs146395561
NM_014908.3(DOLK):c.1129C>T (p.Arg377Cys)
NM_014908.3(DOLK):c.1139G>A (p.Arg380His)	rs553112177
NM_014908.3(DOLK):c.1149T>C (p.Pro383=)	rs1554826752
NM_014908.3(DOLK):c.114A>G (p.Val38=)	rs142000757
NM_014908.3(DOLK):c.1165C>T (p.Arg389Trp)
NM_014908.3(DOLK):c.1222C>G (p.His408Asp)	rs387907030
NM_014908.3(DOLK):c.1241G>A (p.Gly414Asp)	rs1554826737
NM_014908.3(DOLK):c.1257C>G (p.Ile419Met)
NM_014908.3(DOLK):c.1262T>C (p.Leu421Pro)
NM_014908.3(DOLK):c.1286A>G (p.Lys429Arg)	rs574562542
NM_014908.3(DOLK):c.1303G>C (p.Ala435Pro)	rs1306365829
NM_014908.3(DOLK):c.1314C>T (p.Leu438=)	rs148118523
NM_014908.3(DOLK):c.1322A>C (p.Tyr441Ser)	rs137853110
NM_014908.3(DOLK):c.1324G>A (p.Ala442Thr)	rs143641133
NM_014908.3(DOLK):c.1333C>A (p.Leu445Met)	rs866088033
NM_014908.3(DOLK):c.1357G>C (p.Val453Leu)
NM_014908.3(DOLK):c.1373G>T (p.Gly458Val)
NM_014908.3(DOLK):c.137C>T (p.Ala46Val)	rs1554826859
NM_014908.3(DOLK):c.1394G>A (p.Arg465His)	rs148930043
NM_014908.3(DOLK):c.1438A>G (p.Ile480Val)	rs144209926
NM_014908.3(DOLK):c.1446G>A (p.Ala482=)	rs201027607
NM_014908.3(DOLK):c.1450A>G (p.Ile484Val)	rs147630977
NM_014908.3(DOLK):c.1462G>T (p.Ala488Ser)
NM_014908.3(DOLK):c.1481A>G (p.Asp494Gly)	rs145292760
NM_014908.3(DOLK):c.1532G>A (p.Ser511Asn)	rs1178866364
NM_014908.3(DOLK):c.1558A>G (p.Thr520Ala)
NM_014908.3(DOLK):c.159C>G (p.Ala53=)	rs199857223
NM_014908.3(DOLK):c.164A>G (p.Tyr55Cys)
NM_014908.3(DOLK):c.186G>A (p.Arg62=)	rs148171062
NM_014908.3(DOLK):c.192A>G (p.Leu64=)	rs563156233
NM_014908.3(DOLK):c.194A>G (p.Gln65Arg)	rs754744977
NM_014908.3(DOLK):c.1dup (p.Met1fs)	rs531969689
NM_014908.3(DOLK):c.206C>T (p.Ala69Val)	rs1554826850
NM_014908.3(DOLK):c.288G>C (p.Lys96Asn)
NM_014908.3(DOLK):c.292C>T (p.Arg98Trp)
NM_014908.3(DOLK):c.295T>A (p.Cys99Ser)	rs137853109
NM_014908.3(DOLK):c.2T>C (p.Met1Thr)	rs587777137
NM_014908.3(DOLK):c.313C>A (p.Pro105Thr)
NM_014908.3(DOLK):c.344C>T (p.Ala115Val)	rs146804211
NM_014908.3(DOLK):c.376T>G (p.Ser126Ala)	rs1564546286
NM_014908.3(DOLK):c.379G>A (p.Val127Met)
NM_014908.3(DOLK):c.3G>A (p.Met1Ile)	rs1564546510
NM_014908.3(DOLK):c.401G>A (p.Arg134His)
NM_014908.3(DOLK):c.407T>C (p.Val136Ala)	rs1306944564
NM_014908.3(DOLK):c.412A>G (p.Thr138Ala)
NM_014908.3(DOLK):c.429C>G (p.Ile143Met)	rs1261719011
NM_014908.3(DOLK):c.525T>G (p.Val175=)	rs200278288
NM_014908.3(DOLK):c.52G>A (p.Gly18Arg)	rs777998210
NM_014908.3(DOLK):c.560G>A (p.Arg187His)	rs377658203
NM_014908.3(DOLK):c.560G>T (p.Arg187Leu)	rs377658203
NM_014908.3(DOLK):c.572C>A (p.Pro191His)	rs767965852
NM_014908.3(DOLK):c.579G>A (p.Glu193=)	rs28365522
NM_014908.3(DOLK):c.611T>C (p.Val204Ala)	rs1554826810
NM_014908.3(DOLK):c.631C>T (p.Arg211Cys)	rs145310298
NM_014908.3(DOLK):c.633C>T (p.Arg211=)	rs147647278
NM_014908.3(DOLK):c.671A>T (p.Asp224Val)	rs17485436
NM_014908.3(DOLK):c.700A>G (p.Met234Val)	rs139787271
NM_014908.3(DOLK):c.703G>A (p.Val235Ile)	rs759019995
NM_014908.3(DOLK):c.725G>A (p.Ser242Asn)	rs876657786
NM_014908.3(DOLK):c.731dup (p.Phe245fs)
NM_014908.3(DOLK):c.767C>T (p.Ser256Phe)	rs1186154711
NM_014908.3(DOLK):c.771C>T (p.Ile257=)	rs147416890
NM_014908.3(DOLK):c.807T>C (p.Gly269=)	rs769294980
NM_014908.3(DOLK):c.863_865delTTC	rs773789842
NM_014908.3(DOLK):c.873C>T (p.Leu291=)	rs148646968
NM_014908.3(DOLK):c.898C>T (p.Leu300Phe)	rs371529625
NM_014908.3(DOLK):c.912G>T (p.Trp304Cys)	rs1564545929
NM_014908.3(DOLK):c.914C>G (p.Ser305Cys)
NM_014908.3(DOLK):c.931G>T (p.Ala311Ser)	rs1554826773
NM_014908.3(DOLK):c.971_974delinsT (p.Ser324_Ser325delinsPhe)	rs1554826767
NM_014908.3(DOLK):c.975C>A (p.Ser325=)	rs149462670

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